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Synthesis and properties of (1-methylallyl)- and 2-butenyl-silanes

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Bulletin of the Academy of Sciences of the USSR, Division of chemical science Aims and scope

Summary

  1. 1.

    It has been shown that in the Grignard-Wurtz synthesis of alkenylsilanes from 1-bromo-2-butenes, the latter undergo the same type of allyl rearrangement as in the synthesis of hydrocarbons, i.e., in the condensation of R- MgX

    are formed. When R-X is condensed with

    is formed.

  2. 2.

    Silicon analogs of olefins have been synthesized: (1-methylallyl)silane, 2-butenylsilane, methyl(1-methylallyl)silane, trichloro(1-methylallyl)silane, triethyl(1-methylallyl)silane, and trimethyl-3-pentenylsilane.

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Literature cited

  1. A. D. Petrov and V. F. Mironov, Prog. Chem., 4 (1953).

  2. A. D. Petrov and G. I. Nikishin, Bull. Acad. Sci. USSR, Div. Chem. Sci., 1952, No. 6, 1128.

  3. W. Joung, J. Roberts, H. Wax, J. Am. Chem. Soc., 67, 841 (1945).

    Google Scholar 

  4. F. Whitmore, et. al., J. Am. Chem. Soc., 68, 475 (1946).

    Google Scholar 

  5. Yu. P. Egorov and P. A. Bazhulin, Proc. Acad. Sci. USSR, 88, No. 4, 647 (1953).

  6. A. D. Petrov and V. A. Ponomarenko, Proc. Acad. Sci. USSR, 90, 387 (1953).

    Google Scholar 

  7. F. Whitmore, L. Sommer, J. Am. Chem. Soc., 68, 481 (1946).

    Google Scholar 

  8. A. V. Topchiev, N. S. Nametkin, and A. A. Shcherbakova, Proc. Acad. Sci. USSR, 86, No. 3, 889 (1952).

    Google Scholar 

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Petrov, A.D., Ponomarenko, V.A. & Boikov, V.I. Synthesis and properties of (1-methylallyl)- and 2-butenyl-silanes. Russ Chem Bull 3, 429–434 (1954). https://doi.org/10.1007/BF01167821

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  • DOI: https://doi.org/10.1007/BF01167821

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